Submitted an IND to TFDA for a phase II clinical trial on a broad-spectrum antiviral siRNA developed jointly by Microbio (Shanghai) Co.,Ltd. and Oneness.

SEQ_NO	1	Date of announcement	2023/06/09	Time of announcement	17:45:33
Subject	Submitted an IND to TFDA for a phase II clinical trial on a broad-spectrum antiviral siRNA developed jointly by Microbio (Shanghai) Co.,Ltd. and Oneness.
Date of events	2023/06/09	To which item it meets	paragraph 53
Statement	1.Date of occurrence of the event:2023/06/09 2.Company name:Microbio (Shanghai) Co.,Ltd. 3.Relationship to the Company (please enter ”head office” or ”subsidiaries”):subsidiary 4.Reciprocal shareholding ratios:NA 5.Cause of occurrence: (1)New drug name or code: SNS812 (2)Purpose: A. Treatment of COVID-19 infection B. Information Website:has not submitted (3)Planned development stages：Phase II clinical trial/ Phase III clinical trial/NDA (New Drug Application) (4)Current development stage: The phase I study of SNS812 has been completed in the US, obtaining comprehensive pharmacokinetic parameters and preliminary validation of its safety in humans. An IND application for the phase II study in treating COVID-19 infection has been submitted to explore the efficacy, safety, tolerability, and pharmacokinetic characteristics of SNS812 in patients with COVID-19. A. File application/approved/disapproved/Each of clinical trials (include interim analysis): Submit an IND application to the TFDA for Phase II clinical trial. B. Once disapproved by competent authority or each of clinical trials (include interim analysis) results less than statistically significant sense, the risks and the associated measures the Company may occur: NA C. After obtaining official approval or the results (include interim analysis) which are statistically significant, the future strategy:NA D. Accumulated investment expenditure incurred: No disclosure of investment expenditure at the moment in consideration of future marketing strategies and to protect the interests of the company and investors. (5) Upcoming development plan: Phase II/ III clinical trial A. Scheduled completion date: The actual schedule will depend on the progress of the TFDA review. B. Estimate responsibilities: SNS812, a broad-spectrum antiviral siRNA for COVID-19, is developed jointly by Microbio (Shanghai) Co.,Ltd. and Oneness. (6)Market: Based on the data published on June 7, 2023, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has infected more than 767 million people worldwide and caused more than 6.94 million deaths. With the occurrence of vaccine breakthrough and repeated COVID-19 infections caused by new variants, it is anticipated that the future new variants will lead to periodic global epidemics. The emergence of the Omicron variant has highlighted not only the rapid mutation rate of the SARS-CoV-2 virus, but also its astonishing global transmission speed. SNS812 has the potential to be an anti-coronavirus drug unaffected by viral mutations, allowing for long-term usage. While the annual number of flu patients worldwide ranges from 10 to 20 million, with up to 40 million during pandemics, Roche’s Tamiflu has generated over $1 billion in annual revenue. However, given the significantly higher infectivity of the SARS-CoV-2 virus, with over 150 million people infected annually and the number of infections continuing to rise, the market for COVID-19 treatments is predicted to surpass that of traditional flu drugs, reaching $16.2 billion by 2031, according to the well-known analytical firm Transparency Market Research. 6.Countermeasures:None 7.Any other matters that need to be specified(the information disclosure also meets the requirements of Article 7, subparagraph 9 of the Securities and Exchange Act Enforcement Rules, which brings forth a significant impact on shareholders rights or the price of the securities on public companies.): (1)On May 31, 2023, an IND application for the phase II clinical trial was submitted to the US Food and Drug Administration (FDA). This phase II clinical trial will enroll participants simultaneously in both the US and Taiwan to expedite the trial’s progress. (2)According to Guidelines by Taipei Exchange on the Material Information Announced by Listed and OTC Companies, new drug development companies shall make public announcement when filing application for clinical trials to domestic or overseas regulatory authorities, receiving approval or disapproval, obtaining the statistical date of endpoints in each clinical trial (including interim analysis), or receiving approval or disapproval on drug license application. (3)It takes considerable time and expenses to develop a new drug of which success can’t be guaranteed. Investors shall bear such investment risk that warrants careful assessment before making investment decisions.